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      Addressing the batch effect issue for LC/MS metabolomics data in data preprocessing

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          Abstract

          With the growth of metabolomics research, more and more studies are conducted on large numbers of samples. Due to technical limitations of the Liquid Chromatography–Mass Spectrometry (LC/MS) platform, samples often need to be processed in multiple batches. Across different batches, we often observe differences in data characteristics. In this work, we specifically focus on data generated in multiple batches on the same LC/MS machinery. Traditional preprocessing methods treat all samples as a single group. Such practice can result in errors in the alignment of peaks, which cannot be corrected by post hoc application of batch effect correction methods. In this work, we developed a new approach that address the batch effect issue in the preprocessing stage, resulting in better peak detection, alignment and quantification. It can be combined with down-stream batch effect correction methods to further correct for between-batch intensity differences. The method is implemented in the existing workflow of the apLCMS platform. Analyzing data with multiple batches, both generated from standardized quality control (QC) plasma samples and from real biological studies, the new method resulted in feature tables with better consistency, as well as better down-stream analysis results. The method can be a useful addition to the tools available for large studies involving multiple batches. The method is available as part of the apLCMS package. Download link and instructions are at https://mypage.cuhk.edu.cn/academics/yutianwei/apLCMS/.

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          Most cited references34

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          Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing

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            HMDB: a knowledgebase for the human metabolome

            The Human Metabolome Database (HMDB, http://www.hmdb.ca) is a richly annotated resource that is designed to address the broad needs of biochemists, clinical chemists, physicians, medical geneticists, nutritionists and members of the metabolomics community. Since its first release in 2007, the HMDB has been used to facilitate the research for nearly 100 published studies in metabolomics, clinical biochemistry and systems biology. The most recent release of HMDB (version 2.0) has been significantly expanded and enhanced over the previous release (version 1.0). In particular, the number of fully annotated metabolite entries has grown from 2180 to more than 6800 (a 300% increase), while the number of metabolites with biofluid or tissue concentration data has grown by a factor of five (from 883 to 4413). Similarly, the number of purified compounds with reference to NMR, LC-MS and GC-MS spectra has more than doubled (from 380 to more than 790 compounds). In addition to this significant expansion in database size, many new database searching tools and new data content has been added or enhanced. These include better algorithms for spectral searching and matching, more powerful chemical substructure searches, faster text searching software, as well as dedicated pathway searching tools and customized, clickable metabolic maps. Changes to the user-interface have also been implemented to accommodate future expansion and to make database navigation much easier. These improvements should make the HMDB much more useful to a much wider community of users.
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              METLIN: a metabolite mass spectral database.

              Endogenous metabolites have gained increasing interest over the past 5 years largely for their implications in diagnostic and pharmaceutical biomarker discovery. METLIN (http://metlin.scripps.edu), a freely accessible web-based data repository, has been developed to assist in a broad array of metabolite research and to facilitate metabolite identification through mass analysis. METLINincludes an annotated list of known metabolite structural information that is easily cross-correlated with its catalogue of high-resolution Fourier transform mass spectrometry (FTMS) spectra, tandem mass spectrometry (MS/MS) spectra, and LC/MS data.
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                Author and article information

                Contributors
                yutianwei@cuhk.edu.cn
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                17 August 2020
                17 August 2020
                2020
                : 10
                : 13856
                Affiliations
                [1 ]GRID grid.24516.34, ISNI 0000000123704535, School of Software Engineering, , Tongji University, ; Shanghai, 201804 China
                [2 ]GRID grid.59734.3c, ISNI 0000 0001 0670 2351, Department of Environmental Medicine and Public Health, , Icahn School of Medicine at Mount Sinai, ; New York, NY 10029 USA
                [3 ]GRID grid.189967.8, ISNI 0000 0001 0941 6502, Department of Medicine, School of Medicine, , Emory University, ; Atlanta, GA 30322 USA
                [4 ]GRID grid.249880.f, ISNI 0000 0004 0374 0039, The Jackson Laboratory, ; Farmington, CT 06032 USA
                [5 ]School of Data Science, The Chinese University of Hong Kong – Shenzhen, Shenzhen, 518172 Guangdong Province China
                Article
                70850
                10.1038/s41598-020-70850-0
                7431853
                32807888
                6c74ae26-b808-4882-a8ac-7ae9601b5e1e
                © The Author(s) 2020

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 3 February 2020
                : 28 July 2020
                Funding
                Funded by: National Key R
                Funded by: FundRef http://dx.doi.org/10.13039/100000002, National Institutes of Health;
                Award ID: U01CA235493
                Categories
                Article
                Custom metadata
                © The Author(s) 2020

                Uncategorized
                data processing,scientific data,computational biology and bioinformatics
                Uncategorized
                data processing, scientific data, computational biology and bioinformatics

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